Senior Research Manager

Tucker Parker Smith Group (TPS Group); San Rafael (CA); On-site; Full time

Job summary

A leading company is seeking a Senior Manager, Real World Evidence Lead to transform real-world data into actionable medical insights. This role involves leading innovative evidence strategies and collaborating with partners to enhance patient care. Ideal candidates will have a strong background in epidemiology and proven experience in the pharmaceutical industry.

Benefits

Medical insurance

Vision insurance

401(k)

Qualifications

• At least 2 years leading epidemiologic research in pharmaceutical setting.
• Advanced degree required.

Responsibilities

• Lead RWE studies aligned with Integrated Evidence Plans.
• Develop protocols for disease understanding studies.
• Collaborate with external partners on research plans.

Skills

Pharmaco-epidemiologic research

Statistical analysis

Real-world data analysis

Communication

Project management

Education

PhD in epidemiology

Master's in Health services research

Tools

SAS

Python

R

Job description

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Tucker Parker Smith Group (TPS Group) provided pay range

This range is provided by Tucker Parker Smith Group (TPS Group). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$90.00/hr - $100.00/hr

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Professional Recruiter | Matching Talent with Opportunity at TPS Group

Senior Manager, Real World Evidence Lead

12-month assignment (potential to extend)

Pay Rate: $90-$100/hour

San Rafael, CA

Are you passionate about transforming real-world data into meaningful medical insights? Our pharmaceutical client is seeking a dynamic and driven leader to join their Medical Evidence Generation team as a Senior Manager, Real World Evidence (RWE) Lead. In this high-impact role, you'll play a key part in shaping the future of patient care by leading innovative evidence strategies and generating insights that inform clinical practice, support regulatory decisions, and enhance understanding of unmet medical needs. If you're ready to make a difference in a fast-paced, science-driven environment, this is the opportunity for you.

Key Responsibilities:

• Lead RWE studies aligned with Integrated Evidence Plans, guided by the Real World Evidence Product Lead.
• Develop protocols and report findings for disease understanding studies (retrospective and prospective), focusing on patient populations, risk factors, treatment patterns, and outcomes measures.
• Support post-marketing activities, including safety and effectiveness studies/registries, and evaluate risk mitigation strategies.
• Collaborate with external partners (academia, CROs) to implement research plans and oversee research processes.
• Design secondary data analyses using the client's clinical and real-world data to inform program strategy.
• Conduct targeted literature reviews on disease epidemiology and contribute to regulatory documents.

Skills Required:

• Proven experience in pharmaco-epidemiologic research within the pharmaceutical industry.
• Strong understanding of statistical analysis, research methods, and study design.
• Expertise in real-world data analysis (EHR, claims, registry) and statistical programming (SAS, Python, or R).
• Familiarity with healthcare data standards (HL7, FHIR), medical terminologies (ICD10), EMRs, and data privacy regulations (HIPAA, GDPR).
• Ability to thrive in a dynamic environment, manage priorities effectively, and collaborate with stakeholders.
• Self-motivated with strong organizational and project management skills.
• Excellent communication skills, both written and verbal, with the ability to convey complex scientific evidence effectively.
• Experience in rare diseases epidemiology or genetic epidemiology is advantageous.

Education and Experience:

• Advanced degree (PhD, MD, or equivalent) in epidemiology, biostatistics, or related field and at least 2 years of experience leading epidemiologic research in the pharmaceutical setting
• Master's degree in a relevant discipline (ie. Health services research, health outcomes research, public health, statistics, or pharmaceutical sciences) with at least 5 years of experience leading epidemiologic research in the pharmaceutical setting

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research and Project Management

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

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